نتایج جستجو برای: drug release rate

تعداد نتایج: 1651239  

Journal: :research in pharmaceutical sciences 0

buccal mucoadhesive systems among novel drug delivery systems have attracted great attention in recent years due to their ability to adhere and remain on the oral mucosa and to release their drug content gradually. buccal mucoadhesive films can improve the drug therapeutic effect by enhancement of drug absorption through oral mucosa increasing the drug bioavailability via reducing the hepatic f...

Journal: :nanomedicine journal 0
a. akhgari nanotechnology research center , school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, iran targeted drug delivery research center, school of pharmauy, mashhad university of medical sciences, mashhad, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی جندی شاپور اهواز (ahvaz jundishapur university of medical sciences) m. hossein rotubati targeted drug delivery research center, school of pharmauy, mashhad university of medical sciences, mashhad, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)

objective(s):the aim of this study was to prepare electrospun nanofibers of celecoxib using combination of time-dependent polymers with pectin to achieve a colon-specific drug delivery system for celecoxib. materials and methods:formulations were produced based on two multilevel 22 full factorial designs. the independent variables were the ratio of drug:time-dependent polymer (x1) and the amoun...

Journal: :iranian journal of pharmaceutical sciences 0
veerendra s. rajpurohit rajendra institute of technology and sciences, hisar road, sirsa-125055, india pankaj rakha rajendra institute of technology and sciences, hisar road, sirsa-125055, india surender goyal rajendra institute of technology and sciences, hisar road, sirsa-125055, india harish durejab department of pharmaceutical sciences, m. d. university, rohtak- 124001, india gitika arorac ncrd’s sterling institute of pharmacy, navi mumbai- 400706, india manju nagpal school of pharmaceutical sciences, chitkara university, solan-174103, india

in order to enhance in vitro dissolution and content uniformity of poorly soluble drug glimepiride by preparing solid dispersions using modified solvent fusion method, solid dispersions of drug were prepared by modified fusion solvent method using peg 6000 and pvp k25 (as carrier). eight batches (f1-f8) were prepared by factorial design (23) by taking three factors i.e. the concentration of: dr...

اکبری, جعفر, سعیدی, مجید, سیاوشیان, فاطمه, عنایتی فرد, رضا, هشترودی, حامده,

Background and purpose: In Situ Gel dosage forms are successfully used as drug delivery systems to control drug release and protect the medicaments from a hostile environment. The aim of this study was to formulate and evaluate in situ oral topical gels of fluconazole based on concept of pH triggered system. Materials and methods: An in situ gel system consisting of carbopol 934, hydroxypropyl...

سعیدی, مجید, اکبری, جعفر, عنایتی فرد, رضا, چاوشیان, امید,

Background and purpose: The gastroretentive drug delivery systems can be retained in the stomach due to low bulk density. This assist in improving the oral sustained delivery of drugs that have an absorption window in a particular region of the gastrointestinal tract. These systems release the drug content before reaching the absorption site and provide optimal bioavailability. Several approach...

For many years, dexamethasone has been used as an anti-inflammatory drug and is still one of the safest glucocorticoids for treating various diseases. Due to the wide range of the side effects of this drug, it is essential to find a suitable delivering system for reduction in dosage with increased effectiveness. Electrospinning is one of the fiber fabrication methods which is widely used to dev...

Journal: :the iranian journal of pharmaceutical research 0
z jaffariazar e damercheli

the aim of this study was preparation and evaluation of ciprofloxacin-containing minitablets for ocular use, in an attempt to obtain prolonged and controlled drug release to the anterior eye segment. following initial studies on ciprofloxacin powder, it was formulated into ocular minitablets. for this purpose, ciprofloxacin along with various amounts of different sustained release cellulose der...

Fatemeh Atyabi Neda Islami Rassoul Dinarvand, Shadi Moghadam

     In this study, microspheres containing estradiol valerate were prepared by solvent evaporation method using poly (glycolide-co-lactide) (PLGA 50:50) and poly (lactide). The effect of different process variables such as polymer type, drugpolymer ratio, stirring rate, volume of internal phase and temperature of external phase on the morphology, particle size distribution, encapsulation effic...

Journal: :nanomedicine research journal 0
mitra amoli diva department of chemistry, payam noor university (pnu), tehran, iran kamyar pourghazi department of novel medical technologies, darupakhsh pharmaceutical co., tehran, iran

objective(s): researchers have intended to reformulate drugs so that they may be more safely used in human body. polymer science and nanotechnology have great roles in this field. the aim of this paper is to introduce an efficient drug delivery vehicle which can perform both targeted and controlled antibiotic release using magnetic nanoparticles grafted ph-responsive polymer.  methods: fe3o4 na...

Ebrahim Vasheghani-Farahani, Fatemeh Atyabi Mohsen Nosrati Soheila Kheradmandnia

Solid Lipid Nanoparticles (SLNs) have emerged as an alternative colloidal carriers for sustained release of lipophilic drugs with poor absorption and water solubility. This manuscript describes the effect of process variables on the production of Solid Lipid Nanoparticles (SLNs) from beeswax and carnauba wax and ketoprofen release from these carriers. It was found that by increasing drug co...

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